Massari F M, De Martini M, Foresti A, Valentini R, Bertoni T, Lotto A
G Ital Cardiol. 1986 Oct;16(10):845-54.
Amrinone is a nonadrenergic, nonglycosidic agent with combined positive inotropic and vasodilator properties. To determine its clinical and hemodynamic effects we treated 14 patients (12 men and 2 women ranging in age from 36 to 78 years, mean 56) with severe chronic heart failure (New York Heart Association functional class IIIa or IVa) not controlled by conventional therapy. Drug administration: 1 mg/Kg intravenous bolus followed by infusion of 10 mcg/Kg/min over 24 hours; in 11 patients, upon termination of long term infusion, oral therapy was begun (100 mg tid) for a period of four weeks. After bolus and during infusion dyspnea, pulmonary and jugular vein congestion, hepatomegaly rapidly improved, and increase of diuresis was noted. All patients responded with a substantial reduction in central venous pressure (CVP 9.64 +/- 5.96----4.79 +/- 5.66 mmHg, P less than 0.01), wedge pressure (WP 26.3 +/- 4.6----19.00 +/- 4.66 mmHg, P less than 0.01), pulmonary and systemic vascular resistances (PVR 212.07 +/- 121.08----127.64 +/- 50.37 dyne. sec. cm-5; SVR 1687 +/- 301----1297 +/- 357 dyne. sec. cm-5; P less than 0.01); these changes were accompanied by an increase of cardiac index (CI 1.96 +/- 0.38----2.84 +/- 0.83 L/Min/m2; P less than 0.01), stroke index (SI 23.43 +/- 5.85----31.64 +/- 8.86; P less than 0.01) and left ventricular stroke index (LVSWI 22.36 +/- 8.45----34.50 +/- 12.29 g.m/b/m2; P less than 0.01). These positive clinical and hemodynamic effects were not maintained in long term therapy. Moreover we observed adverse effects: fever, nausea and vomiting, thrombocytopenia, liver enzyme elevation, tachycardia and ventricular arrhythmias.
good efficacy and tolerability during short term intravenous therapy in emergency conditions; no clinical improvement and sometimes adverse effects in oral long term therapy.
氨力农是一种非肾上腺素能、非糖苷类药物,具有正性肌力和血管舒张特性。为确定其临床和血流动力学效应,我们对14例(12例男性和2例女性,年龄36至78岁,平均56岁)常规治疗无法控制的严重慢性心力衰竭(纽约心脏协会功能分级IIIa或IVa级)患者进行了治疗。给药方法:静脉推注1mg/kg,随后在24小时内以10mcg/kg/min的速度输注;11例患者在长期输注结束后开始口服治疗(100mg,每日三次),持续四周。推注后及输注期间,呼吸困难、肺和颈静脉淤血、肝肿大迅速改善,尿量增加。所有患者中心静脉压(CVP 9.64±5.96----4.79±5.66mmHg,P<0.01)、楔压(WP 26.3±4.6----19.00±4.66mmHg,P<0.01)、肺血管和体循环血管阻力(PVR 212.07±121.08----127.64±50.37达因·秒·厘米⁻⁵;SVR 1687±301----1297±357达因·秒·厘米⁻⁵;P<0.01)均显著降低;这些变化伴随着心脏指数(CI 1.96±0.38----2.84±0.83L/分钟/平方米;P<0.01)、每搏指数(SI 23.43±5.85----31.64±8.86;P<0.01)和左心室每搏作功指数(LVSWI 22.36±8.45----34.50±12.29克·米/平方米;P<0.01)的增加。这些积极的临床和血流动力学效应在长期治疗中未得到维持。此外,我们观察到了不良反应:发热、恶心、呕吐、血小板减少、肝酶升高、心动过速和室性心律失常。
在紧急情况下短期静脉治疗中疗效良好且耐受性较好;口服长期治疗无临床改善,有时还会出现不良反应。